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  • Analytical Chemistry and Spectroscopy  (24)
  • Tardive dyskinesia  (3)
  • 11
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An oxygen transfer from the nitro group to the C=C group, followed by a simple cleavage, afford intense fragments corresponding to o-nitrosothiophenol at m/z 139 and o-nitrosothiophenoxy cation at m/z 138 during mass spectral fragmentations of allyl o-nitrophenyl sulphide. Further, a concerted double oxygen transfer from the nitro group to the sulphur is proposed for the ejection of ṠO2H from the molecular ion of this compound, leading to the quinolinium cation at m/z 130. These processes are supported by the high-resolution data, collision-induced dissociation linked-scan spectra and chemical evidence.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unexpected ortho interaction of the nitro group has been noticed during the mass spectral fragmentations of N-arylidene 2-nitrobenzenesulphenamides, where the molecular ions expel SO2 and N2 both in concerted and stepwise processes. Loss of a hydrogen or the substituent from this fragment leads to a very abundant ion in all the compounds studied. Based on chemical evidence and linked-scan studies, a 1,2-phenylenetropylium cation structure has been postulated for the [M-SO2-N2-H/substituent]+ ion.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 605-608 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ionized 3-methylbutan-2-ol displays four low-energy fragmentations, loss of CH3· and C3H7· and loss of CH4 and C3H8, the latter pair being produced by metastable ion decompositions. The electron-impact, metastable-ion and collision-induced dissociation mass spectra of 13C and 2H-labelled isotopomers have been recorded, together with appearance energy measurements. It was found that the fast (ion source) losses of CH3· and C3H7· involved only simple bond cleavages between C(1) and C(2) and between C(2) and C(3), respectively, and without any positional interchange of isotopes. The loss of C3H8 produces ionized vinyl alcohol containing only C(l) and C(2). The H atoms involved are only those attached to C(1) and C(3). In deuterium-labelled analogues, the deuterium is preferentially located in the propane, e.g. metastable CD3CH(OH)CH(CH3)2 yields predominantly C3H6D2. On the basis of all the observations, it is proposed that low-energy molecular ions can form a stable proton-bridged molecule-radical complex, \documentclass{article}\pagestyle{empty}\begin{document}$ [{\rm HOCHCH}_2 \cdots \mathop {\rm H}\limits^{\rm + } \cdots \mathop {\rm C}\limits^{\rm .} {\rm H}({\rm CH}_3)_2] $\end{document}, and that this key intermediate is responsible for the isotope distribution in propane loss and also for the relatively low importance of the lowest energy dissociation, the simple C(1)—C(2) bond cleavage.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 25 (1990), S. 689-693 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 26 (1991), S. 1019-1022 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The energetics and mass spectral characteristics of a number of [C7H5]+ ions have been examined. No compelling evidence could be found to show that the 2-cyclopropaphenyl cation was produced by loss of bromine from the ionized 2-bromo derivative. It was proposed that the ethynylcyclopentadienyl cation may be the global minimum on the [C7H5]+ hypersurface.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 459-462 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unusual expulsion of ‘SO’ was observed from the molecular ions of substituted diphenyldithiocarbonates under electron impact conditions. An initial aryloxy migration to sulphur followed by further rearrangement is proposed for this process, based on the substituent effects. The diarylthioketone radical-cation structure assigned for the [M - SO] ion was confirmed through the collision-activated dissociation B/E linked-scan spectra.
    Additional Material: 1 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 1184-1188 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Protonated 4,5-diacetoxyphenanthrene and 2,2′-diacetoxybiphenyl dissociate, owing to the interaction of the two acetoxy groups, by eliminating a molecule of acetic acid. This novel proximity effect, which occurs for a fast atom bombardment-produced closed-shell ion, was examined in detail using tandem mass spectrometric methods. This process, which was first observed in the decompositions of acetylated complex natural products such as stentorin and hypericin, may serve as a general process for determining the proximity of hydroxyl groups in polycyclic aromatic compounds.
    Additional Material: 3 Ill.
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  • 18
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is concluded that C3H8O+· formed by dissociation of ionized 2-ethoxyethanol (8) is a mixture of CH3CH2OCH3+· (7) and ·CH2+OHCH2CH3 (2). Formation of 7 and CH3CH2+OHCH3 (12) is attributed to dissociations of species formed by the hydrogen transfers [CH3CH2OCH2+ ·CH2OH] → [CH3CH2OCH2OCH3+· CH2O] → [CH3CH2+OHCH3HCO·]. Production of 7 competes weakly with dissociation to CH3CH2 +OCH2 (13) and to 12. The low abundance of 7 is attributed to the simple dissociation 8 → 13 being both energetically and entropically favored, and a second H-transfer to give 12 being energetically favored. The threshold for forming 7 is 45 kJ mol-1 above that for dissociation directly to 13, so formation of 7 is the first ion-neutral complex-mediated elimination found to have a threshold above that for the competing simple dissociation. The low abundance of 7 also demonstrates that ion-neutral complexes can be intermediates without obviously revealing their presence by direct dissociation. Experimental results suggest that 2 isomerizes to CH3CH2CH2OH+· (5) and then dissociates by eliminating water. Ab initio results support the feasibility of 2 → CH3+OHCH2CH2· (1) and 2 → 5. However, experimental observations suggest that 2 → 1 does not occur. This is attributed to strong competition from dissociation and isomerization to 5. The transition state for 2 → 5 resembles [CH3CH2CH2OH]+·, and a cyclic transition state for 2 → 5 is ruled out. When the ethyl-oxygen bond in 2 is simply lengthened, the charge is initially concentrated on ethyl, but it switches to CH2OH in a curve crossing at an apparent transition state for C—O bond breaking.
    Additional Material: 2 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 29 (1994), S. 11-17 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The neutral counterparts of the C2H7O+ isomers CH3O+ (H)CH3, CH3CH2OH2+ and \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm C}_2 \,{\rm H}_4 \,\, \cdot \cdot \cdot \mathop {\rm H}\limits^ + \, \cdot \cdot \cdot {\rm OH}_2 $\end{document} were studied by neutralization-reionization mass spectrometry. Protonated dimethyl ether and its  - O(D)+ analogue were produced by protonation (deuteration) of dimethyl ether and also generated as a fragment ion from (labeled) ionized CH3OCH2CH(OH)CH3 by loss of CH3CO⋅. It was observed that the dissociation characteristics of the ions and the stability of their neutral counterpart depended on the internal energy of the protonated ether ions. Stable neutral CH3Ȯ(H)CH3 was only produced from energy-rich ions. The classical protonated ethanol ion CH3CH2OH2+ (a) was produced at threshold by the loss of CH3CO⋅. from ionized butane-2,3-diol. Mixtures of a with the non-classical ion \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm C}_2 \,{\rm H}_4 \,\, \cdot \cdot \cdot \mathop {\rm H}\limits^ + \, \cdot \cdot \cdot {\rm OH}_2 $\end{document} (b) were produced by reaction of C2H5+ ions with H2O. As for the protonated ether, only high-energy a and/or b ions yielded stable hypervalent radicals. It is suggested that the stable C2H7⋅O radicals are Rydberg states.
    Additional Material: 6 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 16 (1981), S. 145-146 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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